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Lower risk Food recall · FDA · Published September 5, 2018

Nishimoto Trading Recalls Everyburger Chocolate Cookies Due to Allergen Labeling Issues

Nishimoto Trading recalls Everyburger chocolate cookies (2.32 oz) for partial allergen labeling on nutrition stickers. Consumers should check packaging for 10 or 80-piece cases.

🇺🇸 FDA recall #F-0017-2019FoodNishimoto Trading ›
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Contact the company

Recalling firmWismettac Asian Foods (USA) dba Nishimoto Trading Co Ltd13409 Orden Dr · Santa Fe Springs, CA 90670-6336
✎ GovInfoNow plain-language explainer

What happened, in plain English

Nishimoto Trading is recalling burger-shaped chocolate cookies because the allergen information on the nutrition sticker is incomplete. This could affect people with wheat, milk, or egg allergies who rely on clear labeling to avoid cross-contamination. Read more at govinfonow.com/recall/18693-nishimoto-trading-recalls-everyburger-chocolate-cookies-due-to-allergen-labeling.

Source Summary by GovInfoNow · govinfonow.com/recall/18693-nishimoto-trading-recalls-everyburger-chocolate-cookies-due-to-allergen-labeling · Updated October 6, 2026 · FDA enforcement record: FDA #F-0017-2019

Cite this page

“Nishimoto Trading Recalls Everyburger Chocolate Cookies Due to Allergen Labeling Issues.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18693-nishimoto-trading-recalls-everyburger-chocolate-cookies-due-to-allergen-labeling. Based on FDA recall #F-0017-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0017-2019%22&limit=1).

Why it’s dangerous

The cookies have incomplete allergen information on the nutrition sticker, meaning wheat, milk, and egg allergies might not be clearly visible. This could lead to cross-contamination risks for sensitive individuals who need precise labeling to avoid allergic reactions.

Who’s affected

People who own or use the Everyburger chocolate cookies (2.32 oz) from Nishimoto Trading are most at risk if they have wheat, milk, or egg allergies. The recall affects consumers who rely on accurate allergen labeling to avoid potential cross-contamination.

How to tell if you have this one

Check for the product name 'Everyburger' on the packaging. The cookies come in two pack sizes: 10 pieces per case (2.32 oz) or 80 pieces per case (10 x 2.32 oz).

  • Brand
    Nishimoto Trading
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Packaging

    Look for the product name 'Everyburger' and the net weight of 2.32 oz (66 g) on the packaging.

Where it went and when

Where it was distributed

Distributed in 21 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: not listedWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: yesMSAlabama: yesALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “WA, CO, AL, TN, VA, PA, MD, MN, IL, AZ, MI, OH, MO, TX, OK, AR, NJ, CA, CA, MS, NY, NV” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arizona, Arkansas, California, Colorado, Illinois, Maryland, Michigan, Minnesota, Mississippi, Missouri, Nevada, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Tennessee, Texas, Virginia, Washington.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Sep 5, 201812. FDA classified it Class II: Oct 4, 201823. Published in FDA’s Enforcement Report: Oct 10, 201834. FDA terminated the recall: Nov 5, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

How many units are affected?

The recall affects all units sold in the U.S. by Nishimoto Trading, including both 10-piece and 80-piece cases.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0017-2019 (September 5, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0017-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA